Validation constitutes one of the fundamental operations of GMP, aiming to guarantee the quality, safety and effectiveness of the finished product
As laboratories become increasingly concerned about external audits and regulations, Millipore offers a comprehensive qualification programme to assist with validation procedures. Installation Qualification (IQ) and Operational Qualification (OQ) are carried out on-site by specifically trained Millipore field service engineers, using routinely calibrated equipment. Essential documentation is also provided, to save time and money when developing Performance Qualification (PQ) for your Millipore water purification system.
Additionally, regular preventive maintenance programs are available separately, or as an integral part of the qualification framework.
All actions carried out during qualification of Millipore systems are documented for full traceability, as required by current regulatory standards. Compliance with GLP and cGMP procedures is essential for pharmaceutical companies.
Millipore has extensive knowledge and expertise to help your equipment meet regulatory standards.
